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Expert Review of Respiratory Medicine|August 14, 2023
Diagnosis and management of pulmonary veno-occlusive diseaseSabina Solinas, Athénaïs Boucly, Antoine Beurnier, et al.Molecular Diagnosis & Therapy|February 3, 2025
Identification of Somatic Genetic Variants in Superficial Vascular Malformations by Liquid Biopsy in a Cohort of 88 Patients from a French HospitalFranck Neil El Sissy, Annouk Bisdorff, Alexandre Perrier, et al.NPJ Genomic Medicine|October 17, 2023
uAUG creating variants in the 5'UTR of ENG causing Hereditary Hemorrhagic TelangiectasiaOmar Soukarieh, Emmanuelle Tillet, Carole Proust, et al.Respiratory Research|June 11, 2010
Absence of influence of gender and BMPR2 mutation type on clinical phenotypes of pulmonary arterial hypertensionBarbara Girerd, David Montani, Mélanie Eyries, et al.Prenatal Diagnosis|October 13, 2017
Prenatal molecular diagnosis in RASA1-related diseaseAurélien Palmyre, Mélanie Eyries, Marie-Victoire Senat, et al.Basic and Clinical Andrology|March 18, 2015
In Vitro fertilization failure of normozoospermic men: search for a lack of testicular isozyme of angiotensin-converting enzymeSelima Fourati Ben Mustapha, Florence Coulet, Mélanie Eyries, et al.European Journal of Human Genetics : EJHG|March 12, 2022
Detection of a pathogenic Alu element insertion in PALB2 gene from targeted NGS diagnostic dataMélanie Eyries, Olivier Ariste, Gaelle Legrand, et al.The Journal of Physiology|July 21, 2023
Physiological and pathophysiological roles of the KCNK3 potassium channel in the pulmonary circulation and the heartAnaïs Saint-Martin Willer, Joana Santos-Gomes, Rui Adão, et al.Journal of Neurosurgery|October 3, 2025
Association of PIK3CA mutations with brainstem location in sporadic cerebral cavernous malformationsMartin Planet, Yohan Ducos, Mélanie Eyries, et al.The European Respiratory Journal|January 26, 2020
Familial pulmonary arterial hypertension by KDR heterozygous loss of functionMélanie Eyries, David Montani, Barbara Girerd, et al.Pageof 6